A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018286



Internal ID19107503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142236996..142767091hg38UCSC Ensembl
Innerchr7:141583272..142154515hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38530096
hg18571244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3667856
Samples
Known GenesLOC730441, MOXD2P, MTRNR2L6, PRSS1, PRSS58
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018286
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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